Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12834Generated: October 25, 2026

2-Aminoadamantane hydrochloride → 5-chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

https://huagongshe.com/reaction/12834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminoadamantane hydrochlorideHCID 25331—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acidHCID 2779652—
Reactant2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 2501354758.5%

Reaction Steps

5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid (69 mg, 0.4 mmol, CAS#: 27006-82-2, purchased from Maybridge) was dissolved in a mixture of dry dichloromethane (3.2 mL) and dry DMF (0.8 mL). DIPEA (0.28 mL, 1.6 mmol) and TSTU (145 mg, 0.4 mmol) were added to the above mixture. After the mixture was stirred for 1 h, the appearance of active ester was detected by LC-MS. Then 2-aminoadamantane hydrochloride (75 mg, 0.4 mmol) was added. After another 2 hours water was added and the organic layer was separated. The aqueous layer was extracted twice with dichloromethane. The combined organic phases were dried under vacuum and purified by C-18 reversed phase HPLC with a gradient of 10-100% acetonitrile/water to give 5-chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (72 mg, 58%). Mass spectrum: m/z: 308.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-50e7ad3ab4024b1b8b9a373a9da549ff
Source noteuspto-grants-2010_06